Diatrizoate,
a refractory ionic iodinated X-ray contrast media
(ICM) compound, cannot be efficiently degraded in a complex wastewater
matrix even by advanced oxidation processes. We report in this research
that a homogeneous process, thiourea dioxide (TDO) coupled with trace
Cu(II) (several micromoles, ubiquitous in some wastewater), is effective
for reductive deiodination and degradation of diatrizoate at neutral
pH values. Specifically, the molar ratio of iodide released to TDO
consumed reached 2 under ideal experimental conditions. TDO eventually
decomposed into urea and sulfite/sulfate. Based on the results of
diatrizoate degradation, TDO decomposition, and Cu(I) generation and
consumption during the TDO–Cu(II) reaction, we confirmed that
Cu(I) is responsible for diatrizoate degradation. However, free Cu(I)
alone did not work. It was proposed that Cu(I) complexes are actual
reactive species toward diatrizoate. Inorganic anions and effluent
organic matter negatively influence diatrizoate degradation, but by
increasing the TDO dosage, as well as extending the reaction time,
its degradation efficiency can still be guaranteed for real hospital
wastewater. This reduction reaction could be potentially useful for
in situ deiodination and degradation of diatrizoate in hospital wastewater
before discharge into municipal sewage networks.